Confusarin

Details

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Internal ID 4b79053b-44bd-497d-b6b0-113c2c0f1e15
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 1,5,6-trimethoxyphenanthrene-2,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O5/c1-20-15-11-5-4-9-8-13(19)16(21-2)17(22-3)14(9)10(11)6-7-12(15)18/h4-8,18-19H,1-3H3
InChI Key JHNVCKNCEVZGGC-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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108909-02-0
2,7-Phenanthrenediol, 1,5,6-trimethoxy-
1,5,6-trimethoxyphenanthrene-2,7-diol
CRH455ZW4X
UNII-CRH455ZW4X
1,5,6-trimethoxy-2,7-phenanthrenediol
SCHEMBL5804536
CHEMBL3634642
SCHEMBL29770963
DTXSID801031838
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Confusarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.8515 85.15%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7244 72.44%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6135 61.35%
P-glycoprotein inhibitior - 0.7911 79.11%
P-glycoprotein substrate - 0.9123 91.23%
CYP3A4 substrate - 0.6191 61.91%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.7856 78.56%
CYP2C9 inhibition - 0.8695 86.95%
CYP2C19 inhibition - 0.6087 60.87%
CYP2D6 inhibition - 0.8156 81.56%
CYP1A2 inhibition + 0.9131 91.31%
CYP2C8 inhibition + 0.4615 46.15%
CYP inhibitory promiscuity + 0.5736 57.36%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.5053 50.53%
Eye corrosion - 0.9826 98.26%
Eye irritation + 0.9179 91.79%
Skin irritation - 0.6693 66.93%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4944 49.44%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5947 59.47%
skin sensitisation - 0.8605 86.05%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6821 68.21%
Acute Oral Toxicity (c) III 0.4932 49.32%
Estrogen receptor binding + 0.8986 89.86%
Androgen receptor binding + 0.6895 68.95%
Thyroid receptor binding + 0.7793 77.93%
Glucocorticoid receptor binding + 0.8057 80.57%
Aromatase binding + 0.7818 78.18%
PPAR gamma + 0.7177 71.77%
Honey bee toxicity - 0.9224 92.24%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9563 95.63%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.35% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.23% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.10% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.64% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.24% 94.00%
CHEMBL2535 P11166 Glucose transporter 83.09% 98.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.02% 80.78%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.20% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.79% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.03% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.06% 95.56%

Plants that contains it

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Cross-Links

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PubChem 11983285
NPASS NPC239996
LOTUS LTS0148509
wikiData Q18348703